A rare inherited coagulation disorder: combined homozygous factor VII and factor X deficiency.

Abstract

The combined presence in the homozygous state of more than one recessively transmitted coagulation defect may rarely occur in countries with a high rate of consanguinity. In an Iranian family consisting of two parents (second cousins) and two affected siblings, initial phenotypic analysis led to a diagnosis of mild FX deficiency (10-19% FX activity, 42-54% FX:Ag), and genotyping revealed a new homozygous missense mutation in the corresponding gene (Ser3Cys). As both of the sibs had a severe bleeding history that was not compatible with mild deficiency of FX, further phenotypic analysis revealed the additional presence of severe FVII deficiency (<1% FVII activity; 63-111% FVII:Ag) associated with the homozygous missense gene mutation Cys310Phe. In this kindred, lack of identification of the double coagulation defect might have led not only to incomplete understanding of the clinical phenotype but also to an incorrect prenatal diagnosis.

• Authors: Marzia Menegatti, Mehran Karimi, Isabella Garagiola, PierMannuccio Mannucci, Flora Peyvandi
• Journal: American journal of hematology (Am J Hematol) Vol. 77 Issue 1 Pg. 90-1 (Sep 2004) ISSN: 0361-8609 [Print] United States
• PMID: 15307115 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2004 Wiley-Liss, Inc.

Topics

• Adult
• Blood Coagulation Disorders (diagnosis, genetics)
• Factor VII Deficiency (complications, diagnosis)
• Factor X Deficiency (complications, diagnosis)
• Family Health
• Female
• Genotype
• Homozygote
• Humans
• Iran
• Male
• Mutation, Missense